$ARCT

Arcturus Therapeutics (ARCT) reported Q2 2026 revenue of $3M ($5M for six months) versus $28.3M and $57.7M a year earlier, citing lower recognition tied to the CSL Seqirus collaboration termination process. Net loss was $23.8M ($0.84/share). Cash was $191.5M, with a runway through 2028. Company regained global rights to KOSTAIVE and received a $12M one-time payment. Phase II ARCT-032 enrollment continues, with a Phase III decision expected in Q4 2026.

Arcturus Therapeutics (Nasdaq: ARCT) terminated its sa-mRNA vaccine partnership with CSL Seqirus via a settlement. Arcturus regained global rights to KOSTAIVE (ARCT-154) and other vaccine programs. CSL Seqirus will pay $12m cash, and Arcturus is released from about $16m in R&D credits, totaling about $28m. The deal unwinds a pact valued around $4.3b.

Arcturus Therapeutics Holdings Inc. (ARCT) filed an SEC Form 8-K — Results of Operations and Financial Condition. EX-99.1 2 e665679_ex99-1.htm Arcturus Therapeutics Announces Second Quarter 2026 Financial Results and Pipeline Progress ARCT-032 (CF) Phase 2 study enrollment remains on schedule; the decision to proceed into Phase 3 expected Q4 2026 ARCT-810 (OTC Deficiency) Phase 2 study enrol

Arcturus Therapeutics (ARCT) shares rose 7.84% to $7.43 on Nasdaq after the company said it entered a strategic collaboration with Thermo Fisher Scientific to support Phase 3 development and potential commercialization of ARCT-032 for cystic fibrosis. Thermo Fisher will provide manufacturing, clinical research and commercialization support via its Accelerator platform, with exclusive commercial manufacturing rights if approved.

Arcturus Therapeutics said it selected Thermo Fisher Scientific to support Phase 3 development of ARCT-032, an inhaled mRNA therapy for cystic fibrosis. Thermo Fisher will provide Phase 3 manufacturing and clinical research services, with Phase 3 expected to run via Thermo Fisher’s PPD if Phase 2 is positive. A separate deal could grant exclusive commercial manufacturing rights if ARCT-032 is approved. Arcturus shares were up 12.19% to $7.73.

Arcturus Therapeutics (NASDAQ:ARCT) rose 5.8% premarket after announcing a collaboration with Thermo Fisher Scientific (NYSE:TMO) for late-stage development and commercialization support of ARCT-032, an experimental mRNA cystic fibrosis treatment. Thermo Fisher will provide manufacturing and clinical research services; Arcturus expects to use Thermo Fisher’s clinical research business if mid-stage data are positive and grants exclusive commercial manufacturing rights if approved.

Arcturus Therapeutics Holdings Inc. (ARCT) filed an SEC Form 8-K — Entry into a Material Definitive Agreement. false 0001768224 0001768224 2026-06-26 2026-06-26 iso4217:USD xbrli:shares iso4217:USD xbrli:shares UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 8-K CURRENT REPORT Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Date of Repor

Arcturus Therapeutics Holdings Inc. (ARCT) filed an SEC Form 8-K — Submission of Matters to a Vote of Security Holders. false 0001768224 0001768224 2026-06-05 2026-06-05 iso4217:USD xbrli:shares iso4217:USD xbrli:shares UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 8-K CURRENT REPORT Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Date of Repor

Arcturus Therapeutics highlights the critical role of phased clinical trials in bringing new gene and cell therapies from scientific discovery to patient treatments. The company emphasizes that each phase provides essential insights into safety and effectiveness, supported by ongoing collaborations to advance rare disease solutions and reports on financial standing and pipeline progress. This rigorous approach ensures promising treatments are thoroughly vetted before market entry.

Arcturus Therapeutics Holdings Inc. (NASDAQ:ARCT) discussed its Q4 2025 earnings, reporting an EPS miss. The call focused on the advancement of its mRNA therapeutic candidates, ARCT-032 for cystic fibrosis and ARCT-810 for ornithine transcarbamylase deficiency, highlighting progress in clinical trials and regulatory interactions. The company also provided updates on its partnered COVID-19 vaccine program and its financial position, including a cash runway extended into Q2 2028.